JPH0477722B2 - - Google Patents
Info
- Publication number
- JPH0477722B2 JPH0477722B2 JP60116840A JP11684085A JPH0477722B2 JP H0477722 B2 JPH0477722 B2 JP H0477722B2 JP 60116840 A JP60116840 A JP 60116840A JP 11684085 A JP11684085 A JP 11684085A JP H0477722 B2 JPH0477722 B2 JP H0477722B2
- Authority
- JP
- Japan
- Prior art keywords
- coumaphos
- emulsifier
- bees
- bee
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 claims abstract description 11
- BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 7
- 239000007900 aqueous suspension Substances 0.000 claims description 4
- 241000256844 Apis mellifera Species 0.000 claims 1
- 241001558516 Varroa destructor Species 0.000 claims 1
- 241000895650 Varroa jacobsoni Species 0.000 claims 1
- 241000257303 Hymenoptera Species 0.000 abstract description 13
- 239000003995 emulsifying agent Substances 0.000 description 19
- 239000000203 mixture Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000238876 Acari Species 0.000 description 5
- WGYZMNBUZFHYRX-UHFFFAOYSA-N 1-(1-methoxypropan-2-yloxy)propan-2-ol Chemical compound COCC(C)OCC(C)O WGYZMNBUZFHYRX-UHFFFAOYSA-N 0.000 description 4
- 241000895647 Varroa Species 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 238000009341 apiculture Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- -1 methyl-7-coumarinyl Chemical group 0.000 description 3
- 239000012875 nonionic emulsifier Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 2
- 241000256837 Apidae Species 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000003958 fumigation Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000001593 sorbitan monooleate Substances 0.000 description 2
- 235000011069 sorbitan monooleate Nutrition 0.000 description 2
- 229940035049 sorbitan monooleate Drugs 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
- UPLPHRJJTCUQAY-WIRWPRASSA-N 2,3-thioepoxy madol Chemical compound C([C@@H]1CC2)[C@@H]3S[C@@H]3C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@](C)(O)[C@@]2(C)CC1 UPLPHRJJTCUQAY-WIRWPRASSA-N 0.000 description 1
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
- PZEUTLIKVUEDLB-UHFFFAOYSA-N 2-[[[2-[[6-amino-2-[[2-[[6-amino-2-[[2-[[2-[[2-[[2-[[2-[2-[[1-[2-[[2-[[2-[[2-[[2-[[2-[[6-amino-2-[[2-[[2-[2-[[2-[[2-[(2-aminoacetyl)amino]-3-methylpentanoyl]amino]acetyl]amino]propanoylamino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-3-hydroxybutanoyl]amino]-3-methylbutanoyl]amino]acetyl]amino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]propanoylamino]-4-methylpentanoyl]amino]-3-methylpentanoyl]amino]-3-hydroxypropanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-3-methylpentanoyl]amino]hexanoyl]amino]-5-carbamimidamidopentanoyl]amino]hexanoyl]amino]-3-(carbamoylamino)propanoyl]-(3-amino-3-oxopropyl)carbamoyl]amino]pentanediamide Chemical compound CCC(C)C(NC(=O)CN)C(=O)NCC(=O)NC(C)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(C(C)O)C(=O)NC(C(C)C)C(=O)NCC(=O)NC(CC(C)C)C(=O)N1CCCC1C(=O)NC(C)C(=O)NC(CC(C)C)C(=O)NC(C(C)CC)C(=O)NC(CO)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(C(C)CC)C(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCCN)C(=O)NC(CNC(N)=O)C(=O)N(CCC(N)=O)C(=O)NC(CCC(N)=O)C(N)=O PZEUTLIKVUEDLB-UHFFFAOYSA-N 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 101000656751 Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) 30S ribosomal protein S24e Proteins 0.000 description 1
- SHBUUTHKGIVMJT-UHFFFAOYSA-N Hydroxystearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OO SHBUUTHKGIVMJT-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 229940072106 hydroxystearate Drugs 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000024241 parasitism Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 230000000384 rearing effect Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 229940109850 royal jelly Drugs 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K51/00—Appliances for treating beehives or parts thereof, e.g. for cleaning or disinfecting
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Veterinary Medicine (AREA)
- Biodiversity & Conservation Biology (AREA)
- Animal Husbandry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Materials For Medical Uses (AREA)
- Catching Or Destruction (AREA)
- Fertilizers (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はみつばちにつくダニ、バロアヤコブソ
ニ(Varoa Jacobsoni)の新規な防除方法、なら
びに、0,0−ジエチル0−(3−クロロ−4−
メチル−7−クマリニル)チオホスフエート
(Coumaphos)を含むバロア病(Varoatosis)剤
に関する。
バロア病はダニの1種、バロアヤコブソニ
(Varoa Jacobsoni)によつて惹き起される。こ
のダニは、成虫の状態で、働きばち、雄バチ及び
女王バチに寄生し、成虫になる前の段階では働き
ばち、雄ばちの幼虫及びさなぎに寄生する。ダニ
による直接の被害があるだけでなく、そのために
はちが衰弱し、ビールスや細菌による病気にかか
り易くなる。
この寄生は養蜂界では新しいことであり、しか
もすでに動物界に広く蔓延した状態にある。バロ
ア病は、みつばちの集団を急激に弱らせたり又そ
の多くを死なせたりして、養蜂に甚大な打撃を与
える。更にこれによつて養蜂製品、例えば蜂蜜、
みつろう、ロイヤルゼリー、及びはち毒が直接被
害を受ける。そして又虫媒作物の授粉が減つてし
まうので、みつばちの間接利用面にも悪影響を与
える。この間接利用はみつばちによる直接生産の
10〜15倍以上に達する。
今迄知られていたバロア病の防除法では、はち
の集団を煙でいぶしたり、活性化合物を散布した
りするのでどうしても悪影響が残る。
熱処理したり、又雄ばちの幼虫の巣の蓋をあけ
て機械的に取り除く方法も知られている。
これら公知の方法には、それを実施するのに莫
大な入力を要し、又そのためにはちの集団に大混
乱を巻き起すという欠点がある。
本発明は、処理1回当り、そしてみつばち集団
1個当り、10〜50mgの0,0−ジエチル0−(3
−クロロ−4−メチル−7−クマリニル)チオホ
スフエート(Coumaphos)を同活性化合物100〜
1000ppmを含む水性懸濁液又は乳化液にして、潅
注、滴下、又は散布することを特徴とするバロア
病の防除法に関する。
本発明の処理方法は、4〜20日間、好ましくは
1〜2週間の間隔で2〜3回、産卵養育が低調な
時期、例えば越冬期間又は休養期間に実施する。
1回の処理当り、クマホス(coumaphos)水
性懸濁液又は乳化液の稀釈液30〜60mlをみつば
ちの集団に滴用する。50mlが好ましい。適用は、
潅注、滴下又は散布して行なう。
この処理により、集団当り10〜50mg、好ましく
は15〜30mgのクマホス(coumaphos)が使用さ
れることになる。
稀釈水性懸濁液又は乳化液中の活性化合物の濃
度は100〜1000ppmである。好ましくは200〜
700ppm、特に好ましくは約500ppmである。
活性化合物濃度0.1〜20%、好ましくは10〜20
%、特に好ましくは16%の乳化又は懸濁原液を用
いて、そのまま使用出来る施用形態液を製造す
る。
これらの剤形は、公知の方法、例えば活性化合
物を増量剤、即ち液状溶媒と、適当な場合には表
面活性剤、即ち乳化剤及び/又は分散剤を用いて
混合して製造する。水を増量剤として使用する時
は、例えば有機溶媒を補助溶媒として使用するこ
とも可能である。液状溶媒として適当なものに
は、例えば芳香族化合物、例えばキシレン、トル
エン、又はアルキルナフタレン、塩素化芳香族又
は塩素化脂肪族炭化水素、例えばクロロベンゼ
ン、クロロエチレン又は塩化メチレン、脂肪族炭
化水素、例えばシクロヘキサン、又はパラフイ
ン、例えば石油留分、アルコール、例えばブタノ
ール、又はグリコール及びそのエーテル及びエス
テル、ケトン、例えばアセトン、メチルエチルケ
トン、メチルイソブチルケトン又はシクロヘキサ
ノン、高極性溶媒、例えばジメチルホルムアミ
ド、及びジメチルスルホキシド及び水がある。適
当な乳化剤としては、例えばノニオン性又はアニ
オン性乳化剤、例えばアルキルアリールポリグリ
コールエーテル、アルキルスルホン酸塩、アルキ
ル硫酸塩、アリールスルホン酸塩、及び蛋白質加
水分解があり、分散剤としては、例えばリグニン
亜硫酸廃液及びメチルセルロースがある。
原液散布(atomizing)、液剤散布(sprayig)、
又は燻蒸(smoking)によつて、活性化合物の液
剤でみつばち一匹一匹を、そして巣全体を濡らす
必要はない。
驚くべきことに、クマホス(coumaphos)は
みつばちの成虫及び幼虫の双方に全身的効果を有
する。
即ち、同化合物は、はちの体内に吸収され、そ
の体液を吸うダニに移行する。
この作用の仕方によつて、はち一匹一匹をいち
いち濡らして、体液を吸つているダニに接触させ
る必要がない。このみつばちでの全身作用は、ク
マホス(coumaphos)が温血動物の体外寄生虫
の防除のために使用した時には見られず驚くべき
ことである。
水で稀釈して施用形態の溶液にするための原液
の組成を下記に示す。
実施例 1
クマホス(coumaphos) 20g
乳化剤 Toximui
(アルキルベンゼンスル
ホン酸カルシウム、ノニオン性乳化剤及びメタ
ノールの混合物で、HLB〓親水性/親油性バ
ランス):10〓 7g
乳化剤 Toximui S
(アルキルベンゼンス
ルホン酸カルシウム、ノニオン性乳化剤、メタ
ノールの混合物、HLB:10) 5g
ソルベツソ(solvesso)200
(高沸点石油留
分からのアルキルナフタレン混合物)
100ml以下
実施例 2
クマホス(coumaphos) 16g
乳化剤 368
アルキルアリールポリグリコー
ルエーテル(分子量1165) 9g
乳化剤 NP10
ノニルフエニルポリグリコー
ルエーテル 9g
ジメチルホルムアミド 10g
ソルベツソ(solvesso)200 100ml以下
実施例 3
クマホス(coumaphos) 5g
乳化剤 Atlox
(ポリオキシエチレンエーテ
ル、ポリオキシグリセリド、アルキルアリール
スルホン酸塩の混合物−易水溶性 2g
乳化剤 Atlox 3409
(ノニオン性及びアニ
オン性乳化剤の混合物−水溶性) 4g
溶剤 PC2(高沸点芳香族石油留分)
100ml以下
実施例 4
クマホス(coumaphos) 1g
乳化剤 368 30g
Dowanol DPM
(ジプロピレングリコール
メチルエーテル) 100ml以下
実施例 5
クマホス(coumaphos) 2.5g
乳化剤 368 10g
乳化剤 NP10 10g
ソルベツソ(solvesso)200 20g
Dowanol DPM 100ml以下
実施例 6
クマホス(coumaphos) 2g
乳化剤 368 9g
乳化剤 NP10 9g
ソルベツソ(solvesso)200 16g
Dowanol DPM 45g
水 100ml以下
実施例 7
クマホス(coumaphos) 1g
乳化剤368 10g
乳化剤NP10 10g
ソルベツソ(solvesso)200 10g
Dowanol DPM 100ml以下
実施例 8
クマホス(coumaphos) 1g
乳化剤 Tween80
(ソルビタンモノオレエ
ートHLB:4.3) 8g
乳化剤 Span
(ソルビタンモノオレエート
HLB:15) 4g
N−メチルピロリドン 100ml以下
実施例 9
クマホス(coumaphos) 1g
クレモホール(cremophor)HS15
(ポリオ
キシエチレン600ヒドロキシステアレート)
20g
クロロベンゼン 100ml以下
実施例 10
クマホス(coumaphos) 1g
乳化剤 W
(アルキルアリールポリグリコー
ルエーテル、分子量約853) 90g
ジメチルイソソルビトール 100ml以下
本発明の処理方法により優れた効果を発揮でき
ることは、下記の実験から明らかである。
実施例
指定数のはちのいるみつばち集団を、50mlの
クマホス水性エマルジヨンを滴下して処理した。
5mlの乳化液を、巣の穴一つ一つに滴下した。こ
の実験での乳化液濃度は30ppm、60ppm又は
90ppmである。
5日間隔で3回処理を行なつた。夫々の処理後
に、死んだダニ及びみつばちの数をかぞえた。処
理が終つた所でそのみつばち集団を殺した。はち
の数をかぞえ、なおとりついているダニをはちか
ら洗い落した。
はじめについていたダニの全数をこれによつて
得た。それから、夫々処理した後の、はちおよび
ダニの死亡率を計算した。
市販剤と比較した実験結果を下記の表を示し
た。
市販剤は商品名がFolbexVA
で、実験では指
示書に従つて燻蒸剤として使用した。市販剤に含
まれている活性剤はイソプロピル4,4′−ジブロ
モベンジアートである。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention provides a novel method for controlling Varoa Jacobsoni, a mite that attaches to honeybees, and a method for controlling 0,0-diethyl 0-(3-chloro-4-
Varoatosis agents containing methyl-7-coumarinyl) thiophosphate (Coumaphos). Varroa disease is caused by a species of mite, Varoa Jacobsoni. In its adult state, this mite parasitizes worker bees, male bees, and queen bees, and before it becomes an adult, it parasitizes worker bees, male bee larvae, and pupae. In addition to the direct damage caused by the mites, this weakens the pups and makes them more susceptible to viral and bacterial diseases. This parasitism is new to the beekeeping world, and is already widespread in the animal kingdom. Varroa disease has a devastating impact on beekeeping by rapidly weakening bee populations and killing many of them. Furthermore, this allows beekeeping products such as honey,
Beeswax, royal jelly, and bee poison are directly affected. In addition, pollination of insect-pollinated crops is reduced, which has a negative impact on the indirect use of bees. This indirect use is a substitute for direct production by bees.
Reaching 10-15 times more. Previously known methods of controlling Varroa disease involve smoking the bee population or spraying active compounds, which inevitably have negative effects. Methods of heat treatment and mechanical removal of male wasp larvae by opening the lid of their nests are also known. These known methods have the disadvantage that they require a large amount of input to carry out and therefore cause havoc in the population. The present invention provides 10 to 50 mg of 0,0-diethyl 0-(3
-Chloro-4-methyl-7-coumarinyl) thiophosphate (Coumaphos) with the same active compound 100 ~
The present invention relates to a method for controlling Varroa disease, which comprises irrigating, dropping, or spraying the aqueous suspension or emulsion containing 1000 ppm. The treatment method of the present invention is carried out 2 to 3 times at intervals of 4 to 20 days, preferably 1 to 2 weeks, during periods when spawning and rearing are slow, such as during wintering or resting periods. For each treatment, 30-60 ml of a diluted coumaphos aqueous suspension or emulsion is applied dropwise to the bee population. 50ml is preferred. The application is
This can be done by irrigation, dripping or spraying. This treatment results in the use of 10-50 mg coumaphos per population, preferably 15-30 mg. The concentration of active compound in dilute aqueous suspensions or emulsions is between 100 and 1000 ppm. Preferably 200~
700 ppm, particularly preferably about 500 ppm. Active compound concentration 0.1-20%, preferably 10-20
%, particularly preferably 16%, to prepare ready-to-use application forms. These dosage forms are prepared in known manner, for example by mixing the active compound with fillers, ie liquid solvents, and if appropriate using surfactants, ie emulsifiers and/or dispersants. When using water as extender, it is also possible, for example, to use organic solvents as co-solvents. Suitable liquid solvents include, for example, aromatic compounds such as xylene, toluene or alkylnaphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons such as chlorobenzene, chloroethylene or methylene chloride, aliphatic hydrocarbons such as e.g. Cyclohexane or paraffins such as petroleum distillates, alcohols such as butanol or glycols and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, highly polar solvents such as dimethylformamide, and dimethyl sulfoxide and water. be. Suitable emulsifiers include, for example, nonionic or anionic emulsifiers, such as alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, arylsulfonates, and protein hydrolysates; dispersants include, for example, lignin sulfites. There is waste liquid and methylcellulose. atomizing, sprayig,
Alternatively, by fumigation, it is not necessary to wet each bee and the entire nest with a solution of the active compound. Surprisingly, coumaphos has systemic effects on both adult and larval bees. That is, the compound is absorbed into the body of the bee and transferred to the tick that sucks its body fluid. This way it works, there is no need to wet each bee and bring it into contact with the mites, which are sucking body fluids. This systemic effect in bees was surprisingly absent when coumaphos was used to control ectoparasites in warm-blooded animals. The composition of the stock solution for dilution with water to give an application form solution is shown below. Example 1 Coumaphos 20g Emulsifier Toximui (a mixture of calcium alkylbenzenesulfonate, nonionic emulsifier and methanol, HLB = hydrophilic/lipophilic balance): 10 = 7g Emulsifier Toximui S (calcium alkylbenzenesulfonate, nonionic emulsifier) , mixture of methanol, HLB: 10) 5 g Solvesso 200 (mixture of alkylnaphthalenes from high-boiling petroleum fractions)
100ml or less Example 2 Coumaphos 16g Emulsifier 368 Alkylaryl polyglycol ether (molecular weight 1165) 9g Emulsifier NP10 Nonylphenyl polyglycol ether 9g Dimethylformamide 10g Solvesso 200 100ml or less Example 3 Coumaphos 5g Emulsifier Atlox (mixture of polyoxyethylene ether, polyoxyglyceride, alkylaryl sulfonate - readily water soluble) 2g Emulsifier Atlox 3409 (mixture of nonionic and anionic emulsifier - water soluble) 4g Solvent PC2 (high boiling aromatic petroleum fraction )
100ml or less Example 4 Coumaphos 1g Emulsifier 368 30g Dowanol DPM (dipropylene glycol methyl ether) 100ml or less Example 5 Coumaphos 2.5g Emulsifier 368 10g Emulsifier NP10 10g Solvesso 200 20g Dowanol DPM 100 ml or less carried out Example 6 Coumaphos 2g Emulsifier 368 9g Emulsifier NP10 9g Solvesso 200 16g Dowanol DPM 45g Water 100ml or less Example 7 Coumaphos 1g Emulsifier 368 10g Emulsifier NP10 10g Solvesso 200 10 g Dowanol DPM 100ml or less Example 8 coumaphos 1g Emulsifier Tween80 (sorbitan monooleate HLB: 4.3) 8g emulsifier Span (sorbitan monooleate
HLB: 15) 4g N-methylpyrrolidone 100ml or less Example 9 coumaphos 1g cremophor HS15 (polyoxyethylene 600 hydroxystearate)
20g Chlorobenzene 100ml or less Example 10 Coumaphos 1g Emulsifier W (alkylaryl polyglycol ether, molecular weight approximately 853) 90g Dimethylisosorbitol 100ml or less It is clear from the following experiment that the treatment method of the present invention can exhibit excellent effects. It is. EXAMPLE A population of honey bees of the specified number was treated with 50 ml of coumaphos aqueous emulsion dropwise.
5ml of emulsion was dropped into each hole in the nest. The emulsion concentration in this experiment was 30ppm, 60ppm or
It is 90ppm. Treatments were performed three times at 5-day intervals. After each treatment, the number of dead mites and bees was counted. Once the process was completed, the bee group was killed. I counted the number of bees and washed the mites that were still attached to them from the bees. This allowed us to obtain the total number of mites that were initially attached. Bee and mite mortality rates were then calculated after each treatment. The table below shows the experimental results compared with commercially available agents. The commercially available product has the trade name FolbexVA and was used as a fumigation agent in the experiment according to the instructions. The active agent included in the commercial formulation is isopropyl 4,4'-dibromobendiatate. 【table】
Claims (1)
り、10〜50mgの0,0−ジエチル0−(3−クロ
ロ−4−メチル−7−クマリニル)チオノホスフ
エート〓クマホス(Coumaphos)〓を、同活性
化合物100〜1000ppmを含む水性懸濁液又は乳化
液の形態で、潅注、滴下又は散布することを特徴
とする、みつばちのダニ、バロアヤコブソニの防
除方法。1. 10 to 50 mg of 0,0-diethyl 0-(3-chloro-4-methyl-7-coumarinyl)thionophosphate (Coumaphos) per treatment and per bee population. A method for controlling the honey bee mite, Varroa jacobsoni, characterized in that it is dipped, dripped or sprayed in the form of an aqueous suspension or emulsion containing 100 to 1000 ppm of the active compound.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3420751.1 | 1984-06-04 | ||
| DE19843420751 DE3420751A1 (en) | 1984-06-04 | 1984-06-04 | METHOD FOR CONTROLLING VAROATOSIS IN BEES |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS611609A JPS611609A (en) | 1986-01-07 |
| JPH0477722B2 true JPH0477722B2 (en) | 1992-12-09 |
Family
ID=6237571
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60116840A Granted JPS611609A (en) | 1984-06-04 | 1985-05-31 | Method of preventing bee varoatosis |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4646377A (en) |
| EP (1) | EP0164629B1 (en) |
| JP (1) | JPS611609A (en) |
| KR (1) | KR920005563B1 (en) |
| AT (1) | ATE65362T1 (en) |
| BR (1) | BR8502644A (en) |
| CA (1) | CA1262861A (en) |
| CZ (1) | CZ281583B6 (en) |
| DD (1) | DD241686A5 (en) |
| DE (2) | DE3420751A1 (en) |
| DK (1) | DK169729B1 (en) |
| ES (1) | ES8607694A1 (en) |
| GR (1) | GR851310B (en) |
| HU (1) | HU209044B (en) |
| IL (1) | IL75368A (en) |
| MY (1) | MY100166A (en) |
| PL (1) | PL253785A1 (en) |
| ZA (1) | ZA854166B (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0259506A1 (en) * | 1986-09-06 | 1988-03-16 | Wilhelm Buschack | Apparatus for treating bee diseases |
| DE3538688A1 (en) * | 1985-10-31 | 1987-05-07 | Bayer Ag | METHOD FOR COMBATING PARASITOSIS IN BEES |
| FR2593023A1 (en) * | 1986-01-20 | 1987-07-24 | Peoch Rene | Composition and method for decreasing the aggressiveness of bees |
| WO2000072683A2 (en) * | 1999-05-26 | 2000-12-07 | Bayer Corporation | An improved process for combating parasitosis in bee colonies |
| BR0113952A (en) * | 2000-09-19 | 2003-09-09 | Bayer Healthcare Llc | Antiparasitic gateway for common bee populations |
| US20050095954A1 (en) * | 2003-11-04 | 2005-05-05 | Jose Castillo | Method of controlling pests |
| US7922559B2 (en) * | 2006-07-27 | 2011-04-12 | Cook Ernest C | Compositions and methods for the treatment and management of bee hives and the bees therein |
| US9655346B2 (en) | 2012-08-14 | 2017-05-23 | Andrey Semenov | Forced air pesticide vaporizer |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2208618C2 (en) * | 1972-02-24 | 1984-08-09 | Bayer Ag, 5090 Leverkusen | Ectoparasiticide Formulations |
| US4308627A (en) * | 1980-08-08 | 1982-01-05 | Wallace Melvin W | Process for prevention of chalkbrood disease |
| DE3225493C2 (en) * | 1982-07-08 | 1987-01-02 | Karl Dr. 6380 Bad Homburg Howorka | Means and methods of protecting bees from Varroa jacobsoni |
-
1984
- 1984-06-04 DE DE19843420751 patent/DE3420751A1/en not_active Withdrawn
-
1985
- 1985-05-17 US US06/735,501 patent/US4646377A/en not_active Expired - Lifetime
- 1985-05-25 DE DE8585106465T patent/DE3583540D1/en not_active Expired - Lifetime
- 1985-05-25 EP EP85106465A patent/EP0164629B1/en not_active Expired - Lifetime
- 1985-05-25 AT AT85106465T patent/ATE65362T1/en not_active IP Right Cessation
- 1985-05-29 GR GR851310A patent/GR851310B/el unknown
- 1985-05-31 CA CA000482907A patent/CA1262861A/en not_active Expired
- 1985-05-31 IL IL75368A patent/IL75368A/en unknown
- 1985-05-31 JP JP60116840A patent/JPS611609A/en active Granted
- 1985-06-03 DK DK248785A patent/DK169729B1/en not_active IP Right Cessation
- 1985-06-03 HU HU852149A patent/HU209044B/en unknown
- 1985-06-03 PL PL25378585A patent/PL253785A1/en unknown
- 1985-06-03 KR KR1019850003867A patent/KR920005563B1/en not_active Expired
- 1985-06-03 BR BR8502644A patent/BR8502644A/en unknown
- 1985-06-03 ZA ZA854166A patent/ZA854166B/en unknown
- 1985-06-03 ES ES543833A patent/ES8607694A1/en not_active Expired
- 1985-06-03 DD DD85276973A patent/DD241686A5/en not_active IP Right Cessation
- 1985-06-03 CZ CS853966A patent/CZ281583B6/en not_active IP Right Cessation
-
1987
- 1987-09-29 MY MYPI87002274A patent/MY100166A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1262861A (en) | 1989-11-14 |
| DK169729B1 (en) | 1995-01-30 |
| DK248785D0 (en) | 1985-06-03 |
| US4646377A (en) | 1987-03-03 |
| DE3420751A1 (en) | 1985-12-19 |
| GR851310B (en) | 1985-11-25 |
| JPS611609A (en) | 1986-01-07 |
| HUT38794A (en) | 1986-07-28 |
| KR860000014A (en) | 1986-01-25 |
| IL75368A (en) | 1989-07-31 |
| EP0164629B1 (en) | 1991-07-24 |
| ATE65362T1 (en) | 1991-08-15 |
| CZ281583B6 (en) | 1996-11-13 |
| BR8502644A (en) | 1986-02-12 |
| KR920005563B1 (en) | 1992-07-09 |
| MY100166A (en) | 1990-02-22 |
| CS8503966A2 (en) | 1988-08-16 |
| DK248785A (en) | 1985-12-05 |
| DE3583540D1 (en) | 1991-08-29 |
| EP0164629A1 (en) | 1985-12-18 |
| ES543833A0 (en) | 1986-06-01 |
| DD241686A5 (en) | 1986-12-24 |
| PL253785A1 (en) | 1986-04-22 |
| IL75368A0 (en) | 1985-09-29 |
| ES8607694A1 (en) | 1986-06-01 |
| ZA854166B (en) | 1986-01-29 |
| HU209044B (en) | 1994-03-28 |
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| EXPY | Cancellation because of completion of term |